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. 2020 Jan 28;26(1):49–61. doi: 10.1007/s12253-020-00797-0

Table 1.

NM23-H1 and its M. musculus, D. melanogaster and C. elegans counterparts participate in three main processes linked to the metastatic cascade

Organism Factor Regulated pathways Function and biological role Citation
Migration and invasion Human tumor (e.g. breast, colon, oral, hepatocellular carcinoma and melanoma) cell lines NM23-H1

Rho - Rac1 signaling MAPK/SAPK and PI3K/Akt pathway downregulation

Gelsolin

hPrune

EDG2

MLC

TGFβ

Inhibition of cell motility and invasion

[6770]

[7173]

[28]

[75]

[7677]

[73]

[78]

[79]

D. melanogaster AWD FGFR PDGFR/VEGFR Tracheogenesis and border cell migration

[82]

[84]

M. musculus NM23-M1 Increased incidence of lung metastases in NM23-M1 KO mice prone to develop hepatocellular carcinoma [66]
Proliferation Human breast carcinoma cell line NM23-H1 Suppression of Ras-MAPK signalling through KSR Proliferation

[37]

[104]

C. elegans NDK-1 Activation of Ras-MAPK signaling through KSR Vulval development [99]
Apoptotic engulfment and phagocytosis Human macrophages (primary cell culture) NM23-H1 Phagocytosis of zymosan and IgG-opsonized RBCs [122]
M. musculus bone marrow-derived macrophages NM23-M1 Engulfment of apoptotic thymocytes [122]
C. elegans NDK-1 Apoptotic clearance of embryonic and germ cells

[121]

[122]

Three main processes (cell migration and invasion, proliferation, apoptotic engulfment/phagocytosis) linked to the metastatic cascade where NM23-H1 and its homologs in model organisms play an important role. Biological functions and the molecular background are also indicated if known. Related citations are listed. See details in the text